Abstract |
A simultaneous flow cytometric assay of the nuclear expressed protein product of the c-myc oncogene p62 and deoxyribonucleic acid ( DNA) ploidy in archival paraffin-embedded tumor material was undertaken in 179 patients with colorectal cancer, followed for up to 9 years. DNA ploidy showed a survival advantage for diploid tumors (chi 2(1) = 5.39, p = 0.020) and could be used to further divide patients with Dukes' A tumors (chi 2(1) = 4.87, p = 0.027) and Dukes' C tumors (chi 2(1) = 5.33, p = 0.021). By dividing patients into 2 levels of tumor expression of p62 c-myc, there was a trend for improved survival in patients with low expression (chi 2(1) = 3.65, p = 0.056). A combination of ploidy status and p62 c-myc expression improved upon survival prediction by ploidy alone in providing 3 groups (chi 2(2) = 7.86, p = 0.0197). While these results do not suggest a replacement for the Dukes' staging for prognosis (chi 2(3) = 33.82, p less than 0.00001), they strongly support the concept that enhanced expression of c-myc oncogene is associated with the progression of colorectal cancer.
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Authors | S Rowley, K M Newbold, J Gearty, M R Keighley, I A Donovan, J P Neoptolemos |
Journal | World journal of surgery
(World J Surg)
1990 Jul-Aug
Vol. 14
Issue 4
Pg. 545-50; discussion 551
ISSN: 0364-2313 [Print] United States |
PMID | 2200214
(Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- DNA, Neoplasm
- Proto-Oncogene Proteins
- Proto-Oncogene Proteins c-myc
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Topics |
- Aged
- Colorectal Neoplasms
(genetics, mortality)
- DNA, Neoplasm
(analysis)
- Female
- Flow Cytometry
- Humans
- Male
- Ploidies
- Prognosis
- Proto-Oncogene Proteins
(analysis)
- Proto-Oncogene Proteins c-myc
- Proto-Oncogenes
- Survival Rate
- Time Factors
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